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Cyclobenzaprine hydrochloride

NDC 68071-2471, Cyclobenzaprine hydrochloride, tablet, film coated, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2471
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213324
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2471 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYCLOBENZAPRINE HYDROCHLORIDE7.5 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE]; Muscle Relaxant [EPC]

Package NDCNDC-11Package
68071-2471-16807124710115 TABLET, FILM COATED in 1 BOTTLE (68071-2471-1)
68071-2471-26807124710220 TABLET, FILM COATED in 1 BOTTLE (68071-2471-2)
68071-2471-76807124710721 TABLET, FILM COATED in 1 BOTTLE (68071-2471-7)
68071-2471-96807124710990 TABLET, FILM COATED in 1 BOTTLE (68071-2471-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c68d17e2-2311-8e17-e053-2995a90a565b

Use it

Look up 68071-2471 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2471 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2471. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.